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- Product NDC
- 31720-705
- 11-digit product format
- 317200705
- Labeler code
- 31720
- Product ID
- 31720-705_93632bb9-4d65-8218-e053-2a95a90a2480
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- OCTINOXATE, TITANIUM DIOXIDE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- S+
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2017-08-28
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; TITANIUM DIOXIDE
- Active strength
- 75 mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 31720-705-17 | 31720070517 | 1 TUBE in 1 CARTON (31720-705-17) > 25 mL in 1 TUBE | 1 tube | 2017-08-28 | 0000-00-00 | No | No | Current |